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Building Physician Resiliency Through CREATION Health: A Research Study

Primary Purpose

Burnout, Stress, Well-being

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CREATION
Sponsored by
AdventHealth
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Burnout

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Physician employed by Centura Health or credentialed physician with privileges at Centura Health
  • Adult ≥ 18 years old
  • English language proficiency
  • Able to provide informed consent
  • Resides in the Denver, Colorado area
  • Willing to commit to the timeline of the study

Exclusion Criteria:

  • Plans to reside outside of the Denver, Colorado area within the 8 months

Sites / Locations

  • Florida Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Behavioral Intervention

Arm Description

The study subjects will be recruited for approximately six weeks prior to the projected start date. The participants will attend the two-day weekend retreat. Follow-up assessments will be administered three months and six months after the retreat. The investigators will analyze the data and complete the study one month after the final assessment is administered.

Outcomes

Primary Outcome Measures

Maslach Burnout Inventory - Human Services Survey
The Emotional Exhaustion subscale scores range from 0 to 54. Higher scores indicate worse outcomes. The Depersonalization subscale scores range from 0 to 30. Higher scores indicate worst outcomes. The Personal Accomplishment subscale scores range from 0 to 48. Higher scores indicate better outcomes.

Secondary Outcome Measures

Well-Being Item
The following question will be asked to assess well-being: "How satisfied are you with your life as a whole?" The scores range from 0 to 10. Higher scores indicate better outcomes.

Full Information

First Posted
January 23, 2018
Last Updated
March 28, 2019
Sponsor
AdventHealth
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1. Study Identification

Unique Protocol Identification Number
NCT03413969
Brief Title
Building Physician Resiliency Through CREATION Health: A Research Study
Official Title
Building Physician Resiliency Through CREATION Health: A Research Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Terminated
Why Stopped
Study has been terminated due to recruitment challenges in targeted area.
Study Start Date
March 20, 2018 (Actual)
Primary Completion Date
March 28, 2019 (Actual)
Study Completion Date
March 28, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AdventHealth

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether a standardized application of a physician-oriented CREATION Health curriculum is associated with reductions in burnout and perceived stress and improvements in well-being and empathy
Detailed Description
This is a prospective, non-randomized study of a convenience sample of Centura Health physicians.This study will not include any drugs or devices. The physician-oriented intervention will consist of a two-day weekend retreat that focuses on the application of CREATION Health principles in order to reduce burnout and perceived stress and improve well-being and empathy. There will be one four-hour session about each of the following CREATION Health principles: Choice, Trust, Interpersonal Relationships, and Outlook.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Burnout, Stress, Well-being

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Behavioral Intervention
Arm Type
Experimental
Arm Description
The study subjects will be recruited for approximately six weeks prior to the projected start date. The participants will attend the two-day weekend retreat. Follow-up assessments will be administered three months and six months after the retreat. The investigators will analyze the data and complete the study one month after the final assessment is administered.
Intervention Type
Behavioral
Intervention Name(s)
CREATION
Intervention Description
The physician-oriented intervention will consist of a two-day weekend retreat that focuses on the application of CREATION Health principles in order to reduce burnout and perceived stress and improve well-being and empathy. There will be one four-hour session about each of the following CREATION Health principles: Choice, Trust, Interpersonal Relationships, and Outlook.
Primary Outcome Measure Information:
Title
Maslach Burnout Inventory - Human Services Survey
Description
The Emotional Exhaustion subscale scores range from 0 to 54. Higher scores indicate worse outcomes. The Depersonalization subscale scores range from 0 to 30. Higher scores indicate worst outcomes. The Personal Accomplishment subscale scores range from 0 to 48. Higher scores indicate better outcomes.
Time Frame
12 Months
Secondary Outcome Measure Information:
Title
Well-Being Item
Description
The following question will be asked to assess well-being: "How satisfied are you with your life as a whole?" The scores range from 0 to 10. Higher scores indicate better outcomes.
Time Frame
12 Months
Other Pre-specified Outcome Measures:
Title
Perceived Stress Scale
Description
The Perceived Stress Scale will be used to measure perceived stress. The scores range from 0 to 40. Higher scores indicate worse outcomes.
Time Frame
12 Months
Title
Jefferson Scale of Empathy
Description
The Jefferson Scale of Empathy will be used to assess empathy. The scores range from 0 to 140. Higher scores indicate better outcomes.
Time Frame
12 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Physician employed by Centura Health or credentialed physician with privileges at Centura Health Adult ≥ 18 years old English language proficiency Able to provide informed consent Resides in the Denver, Colorado area Willing to commit to the timeline of the study Exclusion Criteria: Plans to reside outside of the Denver, Colorado area within the 8 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amanda Terry
Organizational Affiliation
Center for CREATION Health Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Florida Hospital
City
Orlando
State/Province
Florida
ZIP/Postal Code
32804
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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Building Physician Resiliency Through CREATION Health: A Research Study

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